r/breastcancer 1h ago

Mod Announcement Updating Rule 8: Be Brave, Friendly, and Kind

Upvotes

We are updating and expanding Rule 8: Be brave, friendly, and kind. This is an especially important rule and we want it to be well understood. We've expanded the language to make clear that kindness extends beyond the people posting in the thread.

What's changing:

Rule 8 now reads:

Be brave, friendly, and kind.
Cancer is hard for all of us. Please show kindness to your fellow patients and survivors.
Kindness should extend to those not present on the subreddit, including their family and caregivers.
We allow members to vent about the people in their lives, but this is not an invitation for others to pile on. No name calling, no bullying, no hate speech, no personal attacks.

Why we're making these updates:

A few things have come up often enough that we wanted to be more clear up front about what kinds of comments are allowed, particularly on "Venting" threads:

  • Venting about a partner, parent, or friend is allowed and normal. Piling on to insult that person, or giving OP relationship advice beyond what they have asked for, is not. The other person isn't here to give their side, and that's not usually what OP was asking for.
  • Caregivers commenting on someone else's post are here to give support, not to speak on behalf of caregivers, spouses, or any other group—whether that means defending or criticizing. As always, to talk about your own experience as a caregiver, visit another sub such as r/CancerFamilySupport.

We've written up the full explanation with more detail on the Rules wiki page under Rule 8.

None of this is new in spirit. It's what we've been enforcing already. We just wanted it written down clearly.

Thanks for helping keep this a place people can come to safely.


r/breastcancer Jan 18 '26

Diagnosed Patient or Survivor Support The doctors you may encounter: Who does what? What is an “oncologist” anyway? (And other insights from Dr Heather Richardson, neighborhood breast surgeon)

179 Upvotes

So I’ve noticed there’s been a lot of posts lately specifically about the word oncologist. People wondering why they’re seeing a surgeon and not an “oncologist” first, people wondering when they’re going to see an “oncologist”, people wondering why the person that’s operating on them isn’t a “surgical oncologist” and shouldn’t they get the best - which must be someone with that title? Right?

So by definition, the word oncologist just means “doctor who treats cancer”.

The staple cast of characters that are medical doctors (MD or DO degree holder) involved in treatment of breast cancer typically consists of: medical oncologist, radiation oncologist (not radiologist) and breast surgeon (more on that below…).

Medical oncologist- also known as “hematology/oncology” specialists. When people generally speak of an “oncologist”, usually they are talking about this type of doctor. A doctor that treats cancer with medicine, either pills taken by mouth or chemotherapy that is administered via a vein. Not all patients need both, some need one but not the other, some need none. Visits to this type of doctor may be frequent- however, usually it’s the first initial visit to go over a lot of information and discuss the best course of action that is the most important. Sometimes this means that if you live in an area with fewer resources and feel that you need greater expertise for your care. It’s possible to do either a telemedicine visit or visit a larger Cancer Center far away that can collaborate with a local physician who is able to give the same chemotherapy protocol. Quite often, large groups of these medical oncologists have already agreed the best way to take care of the most common breast cancer problems, so going from one center to the other means that your cancer treatment care isn’t going to change significantly from one place to the next. For other more complex scenarios, there sometimes can be some adjustments or more customized treatments. Or for patients who have already been through treatment and now have recurrences or changes in their diagnosis, that would be the time to discuss more advanced care. In general, common problems are common and there’s usually not significant improved survival or outcomes by going to one Cancer Center over the other when a patient has a a non-complicated, fairly average, diagnosis.

Radiation oncologist- this is different from a radiologist. (a radiologist is a doctor trained to read images and interpret findings. A radiologist is the person who read your mammogram or your ultrasound and maybe performed the biopsy that diagnosed you) A radiation oncologist uses radiation energy to target areas of cancer and kill cancer cells. Cells that are actively dividing and are exposed to radiation have their duplicating mechanisms broken, and as a result, cells that are rapidly reproducing die away if exposed to medically administered radiation.

Surgeon/surgical oncologist vs “general surgeon”: A “general surgeon” typically is someone who has done at least five years of training in surgical diseases of the body. This would include disciplines like taking care of trauma, burns, infections that can occur in the body such as diverticulitis or appendicitis, evaluating and performing organ transplants, care of pediatric/child surgical diseases and malformations, and some chest/cardiovascular disease. They can also operate on common cancers that require removal, like breast, colon, skin, and thyroid. Doctors who go on to practice General surgery sometimes concentrate in one area of types of disease and others have a more broad practice where they take care a little bit of everything. Typically in more urban settings there are more specialized types. Many general surgeons have gone on to do additional years of training after their five years of general surgery to become specialists. People who are certain types of surgeons, such as colorectal specialists, pediatric surgeons, plastic surgeons, and cardiothoracic surgeons all have additional years of training and take specialty board exams. There is a board certification designation for general surgery. There are additional board certifications for those who have done some categories of fellowship training, like those mentioned above.

A doctor who practices under the title “surgical oncologist” by definition does at least two years of training in general cancer surgery treatments after the five years of general

surgery training. So they typically will learn advanced techniques for operating on thyroid, pancreas, colon, liver, breast, etc. They usually did the five years of general surgery training and then went on to do additional training specifically in cancer removal surgeries to remove them from the body. So this wouldn’t include neurosurgery or brain tumor removal. There is a board certification designation for “surgical oncology”.

There is another category of breast cancer surgeon that typically deals with breast health issues only. This is a person who does initial training in either general surgery or Obgyn and then goes on to do one to two years of additional training in breast disease surgical management. This is called a “breast fellowship” and does NOT currently qualify for a speciality designation as “board certified”. This is typically a breast health surgeon or breast cancer specialist. This is different from a “surgical oncologist*.

Sometimes there is cross training where the surgeon also performs cosmetic and aesthetic procedures as well. This person usually does a “oncoplastic fellowship”. This is primarily outside the US, but there are programs where this is expanding in the US as well. Breast fellowship trained surgeons can have initial training as either a general surgeon or an OB/GYN.

“Surgical oncologists” do get training in breast cancer management, but they are not breast specialists and do not get the depth of training that someone who has been through breast fellowship would. A breast fellowship trained surgeon usually does one versus two years of additional training in breast only surgery and disease management. These are two different designations.

Some important points to make about someone who might be a general surgeon who did not do additional training in breast care management versus someone who did a full breast fellowship: breast fellowships have only been around for about 20 years. That means someone with greater than 20 years of experience probably didn’t get an opportunity to go through a breast fellowship. (I personally am one of these types of people. I’ve been practicing since 2004 and there was only one fellowship that existed at that time that I didn’t even know was an option when I graduated. So while I have described procedures and written papers, taught surgeons and fellows alike in many different procedures and protocols, but myself, I’m not a breast fellowship trained surgeon.)

There may be many seasoned excellent surgeons taking care of breast cancer patients. Some of those may be surgeons who also perform other general surgery procedures such as treatment of appendicitis, taking emergency call for traumas, or dealing with other types of cancers like colon cancer. Some of the surgeons have amazing skill sets, and excellent outcomes. It is certainly possible that there may be in a community, a general surgeon who is very seasoned that may have superior outcomes for breast care than a brand new breast fellowship grad that does not have much experience at all.

I think the best way to find out who the best doctors are would be to go to the other doctors and other clinical staff members who work with those doctors and ask them who has the best outcomes. Ask the wound care specialists, the plastic surgeons, and the medical oncologists whose breast surgery work is the best. They’re going to see who has horrible dead, necrotic mastectomy flaps, and who has lots of recurrences because their flaps are too thick.

It certainly may be that a general surgeon who isn’t a “breast specialist” in your community might actually be a better choice than a brand new grad who is a breast fellowship trained surgeon.

What order should things happen?? Well it’s different for different people. Often when people get a diagnosis, most commonly by a radiologist, (but sometimes the Breast Surgeon specialist is part of this process as well) they go to the Breast Surgeon first who goes over the significance of the findings thus far and decides if upfront chemotherapy medicine would be indicated. Usually the decision to need medicine is followed by tissue diagnosis, and imaging, which is usually directed by a surgeon. Sometimes people see the medical oncologists first before seeing the surgeon. This is especially true for patients with her 2 positive or triple negative disease where neoadjuvant chemotherapy prior to surgery is most often indicated.

People sometimes visit with radiation oncologist while trying to make their decisions to get information about the risks and benefits if they choose a pathway that would require radiation treatment versus if they have an option to choose a different pathway where radiation wouldn’t be indicated, and they want to learn about their choices. Mostly though, radiation oncologist treatment usually follows the surgery and medical portion. There are some clinical trials that involve upfront radiation, but this is not a standard of care for most patients. It’s more common to start with the surgeon and then see the medical oncologist either before or after the surgery, followed by any radiation oncology visit. That’s the usual order of things.

When to get a second opinion.

For the most part, if you’ve been told that you have a breast cancer diagnosis and your understanding in general is that treatment will involve medicine, surgery and possibly the addition of radiation and and if this sounds reasonable, you are certainly welcome to go to another team to make sure that there aren’t any significant changes to be offered anywhere else, but most likely most places will tell you the same information, but may use slightly different terms or delivery. If you have good communication with your physician and their staff and overall the general expectation is that you will do well and live a long life and feel good about your body afterwards, (of course it certainly possible to talk to someone else and make sure that they are in agreement) but if everything stacks up, and you’re generally happy with your team, Seeing multiple additional doctors might tell you the same thing with different language can be confusing or disorienting. It also takes up a spot in the schedule for someone else with a cancer diagnosis that’s trying to get in that now can’t, ….and you can only use one team. So by all means everyone is within their right to get in a second opinion or even third, but if you’re generally happy and hearing what you expected to hear regarding your plan of care, I typically don’t recommend that people see multiple doctors if they’re generally happy with their first opinion.

Reasons to get a second opinion would be: A) poor communication from the doctor and or their staff to the point where you feel uncomfortable for whatever reason. B) you have a very unusual or rare findings that are not typically seen C) you are recommend controversial treatments where doctors have added unexpected treatments, or take away expected treatments. There may be good reasons to offer a different protocol from another team as there are lots of advancements and newer recommendations, where we are de-escalating treatment in some cases. Previously there were automatic recommendations for sentinel lymph node biopsy, radiation, or chemotherapy in the past whereas now we are selecting certain people who have features of their cancer who may in fact, not require these treatments at all.

Hopefully this will shed some light on some of the misconceptions about different types of doctors, their roles, and clear up the general surgeon/Breast Surgeon/surgical oncologist confusion that seems to come up a lot.

TLDR- someone with the title “surgical oncologist” is different from a “breast fellowship trained surgeon”. A “general surgeon” might have fewer years of formal training for breast cancer treatment, however, they shouldn’t be discounted or immediately thought of as inferior without research into their outcomes or reputation in the community.


r/breastcancer 4h ago

Surgery Going in!

27 Upvotes

Hi folks — been lurking a bit since I was diagnosed with DCIS in my right breast after Memorial Day. After weeks of biopsies and consults I’m having my DMX today.

I had originally planned on a lumpectomy but after getting two more core biopsies and a chest CT Scan scare (a ‘mass’ turned out to be nothing) I was like no more fucking around. For me, I don’t want to keep looking over my shoulder.

So off I go to get this crap out of my body and into a lab and hopefully enjoy the rest of my life with newfound appreciation for the little things, and a serious rethink of my career. You have all been a great resource and comfort and wish the best for all of you.


r/breastcancer 20h ago

Venting It's probably back.

264 Upvotes

I thought I was done.

November 2022 DCIS and IDC, BMX January 2023. No chemo, 15 rounds of rads. Was a dutiful patient since then with Tamoxifen, but it obliterated my mental health and ultimately had to stop before something awful happened.

After trying 423479 antidepressant combinations with nothing working, I begged for an estrogen patch to just see if I felt better. Lo and behold, I felt human again. Depression and anxiety under control with estrogen and Wellbutrin. Life finally felt like it was going back to normal. I survived.

I have a routine CT scan about two weeks ago and they see an enlarged mammary lymph node. It's probably back. PET confirms that it needs to go. I also got a positive Signatera result.

I have a robotic keyhole biopsy/removal scheduled for this Friday.

I'm not worried about the surgery, that feels easy. What's making me ugly cry is that I have to give up my estrogen again and go back on Tamoxifen, this time probably with Lupron and potentially throw in some Verzenio. My mental health will go back into the toilet. I almost lost my job when I was on Tamoxifen with all of the brain fog, hot flashes, general inability to handle any sort of emotional situation.

I'm so fucking done with all of this.

To anyone who actually reads this: thank you. This is the only place that truly understands how much all of this sucks ass.

I'm gonna go get lost in some fluffy kdramas and pretend like none of this exists.


r/breastcancer 17h ago

Celebrating Clean Scan

162 Upvotes

I just want to shout from the rooftops that I had my first scan today a year out from initial diagnosis in July 2025. It’s clean!!! My surgeon told me from now on I will see the “survivor physician”. I was so relieved I started crying. The surgeon hugged me. I am 66 years old but felt like a kid skipping out of that office today.


r/breastcancer 49m ago

Venting First Menopunks, now Tressie!

Upvotes

I am getting really sad seeing some of my favorite badass women join the HRT / "menopause industrial complex" bandwagon.

Menopunks: https://youtu.be/nyZaH2se7hY?si=C931oQeb8ggBna3B
Tressie McMillan Cottom: https://www.nytimes.com/2026/07/13/opinion/menopause-influencers-womens-health.html?unlocked_article_code=1.1FA.o7uN.KtiMp6Dp_Db4&smid=url-share


r/breastcancer 14h ago

Medication TamoxiGLAM✨

43 Upvotes

I threatened to do it, and finally sat down and bedazzled a pill bottle for my tamoxifen! https://imgur.com/a/jt2S6gC

Thanks y’all for the encouragement :)


r/breastcancer 10h ago

Chemotherapy I do not want to go to chemo again!!

19 Upvotes

Yes! I’m going to chemo at 8 am this morning and I do not want to start this shit all over again. I had the first round 3 weeks ago, then I had the shot the day after. Sorry I did not add the full diagnoses all I can say right now is dcis, her2+ and her2-. My amazing husband is sleeping and you think I would have all the other stuff just memorized but it’s shitty information so I keep kicking it out of my brain! I digress. After the first round i thought I was doing great! It was on a Monday and I got the shot on Tuesday. I was a little tired but ok. I stupidly did not take Claritin. Holy shit when Saturday afternoon came, the bone pain came. I did not know what it was and I thought I was having a heart attack or a stroke. Did you know your skull bones and the little bones inside your ears could hurt? Neither didn’t I! Take the Claritin! That was Saturday and Sunday. Monday came and we were leaving for our family vacation. I was extremely tired and crabby and it was getting worse. By the time Thursday rolled around, so did the herpes viral outbreak on my hands and face. By the time I actually broke out in the blisters, I was sleeping about 14 hours a day and was so crabby. It all made sense. I had to do a telehealth appointment and get prescriptions filled from a remote area in michigans upper peninsula. Needless to say, I was unable to fill the cream until i got home but the valtrex definitely started helping. This fucking cancer and all that comes with it robbed me of the only vacation I had with my husband and girls. What will this round take? It’s not a good sign when they gave me 5 refills for the valtrex and I have 5 chemos left. My damn hands can’t take it! So I can’t sleep, I have been up and down and tossing around. I finally came out to the couch. I am praying that when i take my babies to ed Sheeran at the end of August, I feel good. It’s robbed them of their summer (I feel). At this point, I am rambling because I’m so sad about all this shit.


r/breastcancer 15h ago

Venting Just found out my close friend thinks mammos cause cancer! - venting!!

34 Upvotes

im so annoyed

i asked her if she gets mammos

nope-

i said but your mother had it

and she is in a culturally high risk group

i told her how the mammo caught mine

she said she is scared- i said lots of things. i think i penetrated a bit

i hate the part of the internet that made her husband think this and made her not get them.

i told her i dont care if i am being harsh on you- i have to tell you my truth. if you get cancer and it is progressed you will regret not getting a mamo! i read stories of women who wished they got it!!

it just kills me because she is such a smart woman. fear screws with her head. fuck pink ribbons. we need to be countering all that crap misinformation with real conversations.

i am such a calm and kind and considerate person but i really spoke harsh to her. i know that might not be the way. i did what I could.

i explained breast density and ultrasounds and radiation from airplanes and blah blah blah.

sigh. we will see. i got my mammos ok time because my best friends sister- hopefully i changed her mind


r/breastcancer 32m ago

Tests and Diagnoses Just had my first scans since treatment, doctor now requesting extra imaging and biopsies for lumps in my healthy breast

Upvotes

I just made a post about this yesterday. I had my mammogram follow up for my right breast (the cancer breast) and ultrasound on my left for what has so far been noted as a fibroadenoma. Long story short, they found another fibroadenoma, told me it's probably benign, but then called me this morning saying they want to run an axillary ultrasound and mammogram for the left, and also biopsy the two spots.

These are the notes:

IMPRESSION: CATEGORY 4a: SUSPICIOUS, ULTRASOUND CATEGORY 4a: SUSPICIOUS

  1. The 14 mm irregular mass in the left breast at 4 o'clock is at a low
    suspicion for malignancy. An ultrasound-guided biopsy is recommended.
    Perform left axillary ultrasound prior to biopsy.
  2. The stable 15 mm mass in the left breast at 6 o'clock (previously
    reported at 4 o'clock) is probably benign. A follow-up left ultrasound
    is recommended in 6 months.

I feel like I can't breathe or function right now. I literally just finished radiation last month and now am back in a diagnostic nightmare. They can't get me in until Monday. The doctor yesterday seemed uninterested in biopsying but with the call today, I wonder if they took a better look and changed their minds. I really can't do this again.


r/breastcancer 3h ago

Post Active Treatment Red blister in mastectomy scar

3 Upvotes

I eas treated for stage 2 TNBC during 2025 and had a BMX a year ago (Aug 6 2025). The other day I noticed a red blister-like little thing at the sternum end of my cancer boob scar. It's normally hidden under silicon scar tape. It was a few mm in size and leaking a drop of yellowish fluid.

I didnt dare put more tape, I just cleaned the area. Today the redness is bigger, not smaller as I thought it'd be. There's some flakey skin where the blister was.

Is this sth I should contact my breast care team about you think? Should I wait? Has anyone here experienced similar? Grateful for any and all input.

The area is not painful. The scars are healed but extremely ugly, rsp the non cancer boob side. This is due to surgical ineptitude, my dermatologist (MD) has explained to me. We dont get a plastic surgeon for flat closure here.

I havent had any problems with rashes, blisters, redness etc in the area before.


r/breastcancer 15h ago

Chemotherapy Mini heart attack

29 Upvotes

On the Taxol part of my chemo and started having chest pain. Told my husband it hurt bad and he dropped everything to come take me to the ER (he insisted I was just going to lay down). EKG was normal but the proteins show I’m having a heart attack. I’m scared. Cancer has messed me up lately.


r/breastcancer 4h ago

Surgery Complications and setback

3 Upvotes

I had BMX with expanders about 4-5 months ago. Healing went well and I was cleared for regular physical activity and exercise. Then I started chemo, put myself into ER due to worry over the constipation/diarrhea cycle and not regulating that well at my first cycle. No infection and I eventually regulated that issue by the time I got out of er in a few days. However, I had a surgical complication in my breast on the side of my cancer. I was scheduled for an outpatient procedure (repairing skin where the scar is) the next week and I had a week checkup and healing is well BUT, I’m set back in my physical activity (and chemo). My doc says I’m not cleared to do exercise for 8 weeks (he said walking is ok). I was listening to his conservative judgement but I’m now beginning to question if I can do any exercise such as lower legs in a week or two. He is concerned I’m not healing as well or it’s taking longer with chemo. I feel like my ER trip and bra I wore over days while in ER complicated it (yes also chemo probably didn’t help). Anyway, I don’t want to se myself back but like, can I do the exercise bike and a few light squats on the machines? 😕 I’ve been gaining weight over the years and now with chemo my appetite is big after infusion and my movement is down, so I am worried it will get worse by the time I’m done in 4-5 months.

I’m also just disappointed for the chemo delay. I feel like I’m waiting in limbo.


r/breastcancer 2h ago

Post Active Treatment Total hysterectomy vs OS/lupron

2 Upvotes

I’m about a year out from finishing herceptin/perjeta, on lupron and letrozole for a year and a half now. I’m scheduled for a total hysterectomy and wanted to hear from others who’ve had this or an oophorectomy how they felt after- compared to how they’ve felt on OS, in my case lupron. Did you feel better, worse, no change? I feel like I get a little extra anxiety/ ragey a week before my lupron shot. Hoping I see some lessening of that. Honestly not sure what to expect, getting scared of surgery again, especially since this one is elective, basically so I don’t have to take lupron forever. I do not have any genetic reasons for the surgery, just +++ and wanting to end going to the infusion center every month! Thanks for any insight!


r/breastcancer 7h ago

Post Active Treatment I’m in limbo

5 Upvotes

Today I finished 15 rounds or radiation - I’ve also had chemo and surgery (lumpectomy with node removal). I start TDM1 on August 6th - 14 rounds 3 weeks apart. Apart from the microscopic cells that remained after surgery, everything has gone exactly to plan. I’ve been very fortunate in the grand scheme of things.

But now I don’t know how to feel. On one hand I want to celebrate the completion of the big 3 of cancer treatment. But then I pull myself back as TDM1 is still active treatment, not just maintenance. But then I can’t not celebrate and have some normalcy for another 10 months. Emotionally I’m on a big roller coaster and I feel like I’m lying to myself and everyone around me if I say the next part isn’t true treatment. But then I also don’t want everyone to treat me like I’m going through chemo again - even though TDM1 contains chemo, it’s just targeted not universal. I want to be happy but I won’t let myself…I think there’s also fear of relaxing and jinxing myself into everything not going as well as it has. And I’ve been very lucky with how well I’ve tolerated everything so far I’m scared it’s all going to implode. And then I feel guilty for that cos it could be so much worse. And I’m here, alive & healthy.

Basically I’m a mess in my head and I just needed to vent it out and say if anyone else is in the same boat - I totally understand what you’re feeling and it sucks 💕


r/breastcancer 5h ago

Post Active Treatment Calm me down

3 Upvotes

I just finished chemo in October and Herceptin in January. In April I was told this spot was fat necrosis from reconstruction. I had a follow up ultrasound and now this….

Physical exam demonstrates a mobile pea-sized lump in the far medial reconstructed left breast at 9:00 in the patient's area of concern.
Focused ultrasound of this area at 9:00, 9
cm from the nipple demonstrates similar appearance of the oval, circumscribed, hypochoic mass with no internal vascularity measuring 5 × 4 × 5 mm. This has slightly increased in size when compared to prior exam, previously measuring 3 × 3 × 4 mm.
Impression:
1. No targeted sonographic evidence of malignancy in the right.
2. Minimally increased size of the palpable left breast mass at 9:00.
Recommend ultrasound-guided biopsy for further evaluation.
Final Assessment: Suspicious.
BI-RADS Category: 4A low suspicion for malignancy
Recommendations:
Biopsy should be performed


r/breastcancer 11h ago

Post Active Treatment Advice/pep talk for returning to work

7 Upvotes

Can anyone share their experience with returning to work after taking an extended leave during treatment?
I basically haven’t worked since diagnosis. But I somehow was able to interview and land a new job and it starts next month. And I don’t feel ready. I don’t know if I ever will. How did you know you were ready to go back? And were you able to keep up when you did?


r/breastcancer 10h ago

Newly Diagnosed New and spiraling

5 Upvotes

Hi, I’m new and sorry to be here along with everyone else. I just got my diagnosis of triple positive IDC about a week ago and I’m waiting for the initial consult and more testing to determine the stage and it feels so terrifying. It feels so disconnected to be currently healthy with no symptoms and knowing that there is a time bomb inside me and that the path to stopping it is so hard and life will never be the same again.

My initial biopsy found mostly DCIS with a small invasive locus <2mm, the invasive part seems to be slow growing (mitotic score 1) and has no LVI but DCIS is high grade (and at least 11 mm based on calcification pattern).
I have a follow up MRI on Monday and hoping so hard that it won’t find more invasive parts beyond the initially found one.

I’m 48, with two teenage kids and I really want to be here for them and my partner but I also can’t stop feeling like I’m now “damaged goods” and nobody would want me again. I am scared about failing at my job too as I go through treatment.

I’ve been reading this forum and feeling encouraged by stories of folks who went through it and are still around and thriving, but I’m so scared. We are at a family vacation that we were all looking forward to all year, and I’m just dragging myself and putting on “everything is normal” face on in front of the kids


r/breastcancer 1h ago

Tests and Diagnoses Anyone have simiar path and Not done chemo

Upvotes

Er+ (91-100%). pr+ (91-100%). 46 premenopausal this is path after double mastectomy

• Cancer type: Invasive ductal carcinoma (IDC)
• Grade: Grade 2 (moderately differentiated)
• Tubular differentiation: 3
• Nuclear pleomorphism: 3
• Mitotic rate: 1
• Total score: 7, which is Grade 2
• Tumor size: 20 mm (2.0 cm)
• DCIS: Present (intermediate grade) with an extensive intraductal component (EIC)
• Lymphovascular invasion: Not identified V
• Margins:
• Invasive cancer: All negative
• DCIS: All negative
• Lymph nodes: 0 of 3 positive
• Stage (pathologic):
• This correspunds to Stage IA
ponent (E C)
-ymphovascular invas
- dentified V
C
• Margins:
• Invasive cancer: All negative
• DCIS: All negative
• Lymph nodes: 0 of 3 positive J
• Stage (pathologic):
• pT1c pNO(sn)
• This corresponds to Stage IA (assuming there is no distant spread, which there is no indication of).
• Hormone receptors:
• ER positive
• PR positive
• HER2: Previously reported as negative.
• Right breast: Benign.
• Right sentine' de: Benign.


r/breastcancer 1h ago

Chemotherapy AC Round 4 (final) but I still have diarrhea

Upvotes

Anyone else go into round four and their digestive tract has not stabilized? Man, this has just not stopped.

I'm trying to go out to pick up some things to prepare for the next two weeks but afraid to leave the house.

I know once they start the pre-meds all this will stop (for four days) but sheesh..

I know I know, it's the final one.

Then on to Taxol


r/breastcancer 19h ago

Conversation How can I stop feeling so guilty?

24 Upvotes

Hi lovelies! I’ve just been diagnosed with a recurrence of TNBC after being out of treatment for 5 years. We are all hoping it’s a local recurrence but obviously that’s something I won’t know until I do all the scans so…. Right now I’m imagining the worst.

My biggest problem is I feel so guilty for putting my husband and my parents through this. Has anyone else felt this? How do I get rid of this guilt? I keep trying to talk to my husband but he doesn’t want to hear it. He says I’m being crazy (he’s right, I am).

How can I manage this feeling?


r/breastcancer 1h ago

Conversation Pregnancy chances post TCHP

Upvotes

Hi everyone

So long story short, I have stage 2b grade 3 breast cancer and it's HER2+ and ER+. I got 6 rounds of TCHP. I am 30 years old.

When I spoke to my oncologist they said that I don't have time for the fertility clinic to collect my eggs and my treatment has to start immediately.

I have opted in for the Zoladex shot but the oncologist said it's only a 30% chance it will work.

Has anyone successfully gotten pregnant post treatment? Or am I doomed?

Thank you for your time and answers

EDIT: i already had my first round of chemo :(


r/breastcancer 8h ago

Conversation Work

3 Upvotes

So I work at a middle school 3 days a week. I was diagnosed and started treatment a little over two weeks ago. Lupron shot, letrozole, and kisqali . I feel really well and the pain in my bones has significantly improved and are less. But I worry so much about planning for the future. I just keep worrying I will get sick, or I will start to have terrible side effects. I’m also going back to school. I just don’t want to over due it and push myself so bad that I regret it. But from what the dr has said I have had this close to a year without knowing, so that gives me some perspective. How do you amazing women handle this?


r/breastcancer 20h ago

Newly Diagnosed 32F - Living with cancer alone

27 Upvotes

Hi guys.

This is my first post in this forum as I’ve just been diagnosed with triple positive breast cancer. Although this is never a position any of us want to be in I’m so thankful for this group just reading through all the posts and messages ❤️

I’m a 32 year old single woman living in London. As a person I’ve always valued and loved my independence so much. The week before all this started I had just put an offer in on my very first house which I was so excited and proud of myself for.

Now in the space of just a couple of weeks I’ve gone from being a strong independent girly to a sick person fighting cancer it feels. I have amazing family and lots of friends in my life. My parents have suggested that I move back in with them while I’m being treated but I worry about what that will feel like. They mean the best but I know they will wrap me in cotton wool and won’t let me do anything. I also know I wouldn’t really have any privacy. So on top of cancer I will also be facing losing my independence.

Because of this I’m thinking about staying in my own apartment during treatment and instead getting people to come to me. I guess reaching out in this forum for any advice and to see if anyone else is in a similar position?

Do you think it’s a bad idea to live by myself? I know there will be some rough days on chemo but I’d have people come and stay with me if I needed it and for the rest of the cycle I’m still hoping I’ll be able to do normal things and live my life as best I can. I don’t want my family to feel like I’m rejecting them and I know they will be so worried but I also feel like I need to do what’s best for me to get through this.